CAS:53801-63-1 | Zinc-Copper Couple
Name:Zinc-Copper couple
CAS:53801-63-1
Cu(ICP):1%-3%
MDL No:MFCD00084851
Molecular Formula:Zn·Cu
Molecular Weight:128.93
Melting Point:419-420° C
Boiling Point:N/A
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Product Introduction
Name:Zinc-Copper couple
Synonyms:Copper, compd. with zinc;
CAS:53801-63-1
Cu(ICP):1%-3%
MDL No:MFCD00084851
Molecular Formula:Zn·Cu
Molecular Weight:128.93
Melting Point:419-420° C
Boiling Point:N/A
Appearance:Grey to black powder
Sensitivity:Moisture Sensitive
Water solubility:Insoluble in water
Storage condition:Store at 4°C. Do not store together with acids. Protect from humidity and water.
Packaging & Delivery
Package:5g/10g/25g/50g/bulk package
Transportation: by FeDex or by ocean shipping or clients requirement
Delivery Detail: Within 3-5 days after full payment
Flexible payment terms: support T/T, Paypal , Credit Card
Application:Zinc-copper couple(CAS:53801-63-1) is used in the Simmons-Smith cyclopropanation reaction, Reformatsky reaction. It is used as a chemical for the selective, stereospecific reduction of alkynes to cis-alkenes. It is used in for deiodination of iodotributylstannylalkanes. In the presence of a free-radical initiator, it promotes the formylation of perfluoroalkyl iodides with DMF to give fluorinated aldehydes in high yield. It is used in dermatology.
Reference:
Eugene LeGoff. Cyclopropanes from an Easily Prepared, Highly Active Zinc—Copper Couple, Dibromomethane, and Olefins.J. Org. Chem.1964, 29 (7), 2048-2050.
S. Morris Kupchan; Masao Maruyama. Reductive elimination of epoxides to olefins with zinc-copper couple.J. Org. Chem.1971, 36 (9), 1187-1191.
For use in the Simmons-Smith cyclopropanation reaction, see Diiodomethane, A15457. For use in the Reformatsky reaction, see: Synthesis, 698 (1977).
Used for the selective, stereospecific reduction of alkynes to cis-alkenes: Chem. Ind. (London), 143 (1957). For deiodination of iodotributylstannylalkanes, see: Synlett., 891 (1992).
In the presence of a free-radical initiator, promotes the formylation of perfluoroalkyl iodides with DMF to give fluorinated aldehydes in high yield: J. Fluorine Chem., 63, 217 (1993).

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